TY - JOUR
T1 - Regulatory role of prostanoids in glomerular microcirculation of remnant nephrons
AU - Nath, K. A.
AU - Chmielewski, D. H.
AU - Hostetter, T. H.
PY - 1987
Y1 - 1987
N2 - The glomerular microcirculation of the remnant nephron is characterized by reduced afferent (R(A)) and efferent (R(E)) arteriolar resistances and markedly increased single nephron glomerular plasma flow and filtration rates. We investigated the role of prostanoid production in mediating these adaptive alterations in glomerular hemodynamics after the reduction of renal mass. Acute administration of indomethacin, 5 mg/kg iv in anesthetized euvolemic, Sprague-Dawley rats with intact kidneys led to no significant alteration in renal hemodynamics, whereas in similarly prepared subtotally nephrectomized rats such inhibition significantly reduced remnant kidney glomerular filtration rate from 0.57 ± 0.07 to 0.45 ± 0.05 ml/min and single nephron glomerular filtration rate (SNGFR) from 93 ± 4 to 72 ± 5 nl/min. This reduction of SNGFR was due to diminutions in the glomerular ultrafiltration coefficient (K(f)) from basal values of 0.061 ± 0.004 to 0.050 ± 0.004 nl·s-1·mmHg-1 and in initial glomerular capillary plasma flow rate (Q̇(A)) from 416 ± 42 to 321 ± 42 nl/min. The decrease in Q̇(A) was a consequence of proportional increases in R(A) and R(E). In other groups of animals we demonstrated that urinary excretions of both vasodilatory as well as vasoconstrictor prostanoids per surviving nephron increase several fold in subtotally nephrectomized rats compared with rats with intact kidneys and that administration of indomethacin, 5 mg/kg iv, reduced urinary excretions of both vasodilatory prostaglandins, prostaglandin E and 6-keto-prostaglandin F(1α), as well as vasoconstrictor prostanoid, thromboxane B2, to the same degrees in both subtotally nephrectomized rats and rats with intact kidneys. We conclude that after the reduction of renal mass adaptive increments in synthesis of both vasodilatory and vasoconstrictor prostanoids occur in surviving nephrons. The hemodynamic effects of prostaglandins on R(A) and R(E) and on K(f) account, at least in part, for the increments in single nephron glomerular plasma flow and filtration rates.
AB - The glomerular microcirculation of the remnant nephron is characterized by reduced afferent (R(A)) and efferent (R(E)) arteriolar resistances and markedly increased single nephron glomerular plasma flow and filtration rates. We investigated the role of prostanoid production in mediating these adaptive alterations in glomerular hemodynamics after the reduction of renal mass. Acute administration of indomethacin, 5 mg/kg iv in anesthetized euvolemic, Sprague-Dawley rats with intact kidneys led to no significant alteration in renal hemodynamics, whereas in similarly prepared subtotally nephrectomized rats such inhibition significantly reduced remnant kidney glomerular filtration rate from 0.57 ± 0.07 to 0.45 ± 0.05 ml/min and single nephron glomerular filtration rate (SNGFR) from 93 ± 4 to 72 ± 5 nl/min. This reduction of SNGFR was due to diminutions in the glomerular ultrafiltration coefficient (K(f)) from basal values of 0.061 ± 0.004 to 0.050 ± 0.004 nl·s-1·mmHg-1 and in initial glomerular capillary plasma flow rate (Q̇(A)) from 416 ± 42 to 321 ± 42 nl/min. The decrease in Q̇(A) was a consequence of proportional increases in R(A) and R(E). In other groups of animals we demonstrated that urinary excretions of both vasodilatory as well as vasoconstrictor prostanoids per surviving nephron increase several fold in subtotally nephrectomized rats compared with rats with intact kidneys and that administration of indomethacin, 5 mg/kg iv, reduced urinary excretions of both vasodilatory prostaglandins, prostaglandin E and 6-keto-prostaglandin F(1α), as well as vasoconstrictor prostanoid, thromboxane B2, to the same degrees in both subtotally nephrectomized rats and rats with intact kidneys. We conclude that after the reduction of renal mass adaptive increments in synthesis of both vasodilatory and vasoconstrictor prostanoids occur in surviving nephrons. The hemodynamic effects of prostaglandins on R(A) and R(E) and on K(f) account, at least in part, for the increments in single nephron glomerular plasma flow and filtration rates.
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U2 - 10.1152/ajprenal.1987.252.5.f829
DO - 10.1152/ajprenal.1987.252.5.f829
M3 - Article
C2 - 3578532
AN - SCOPUS:0023189014
SN - 0002-9513
VL - 252
SP - F829-F837
JO - American Journal of Physiology - Renal Fluid and Electrolyte Physiology
JF - American Journal of Physiology - Renal Fluid and Electrolyte Physiology
IS - 5 (21/5)
ER -